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Canonical Allele Identifier: Get Identifier
Gene: APP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001129602.1:p.Phe635Leu
NM_001136130.3:c.1903T>C

NM_001136130.3:c.1905T>A

NM_001136130.3:c.1905T>G